1k9g
From Proteopedia
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Crystal Structure of the Complex of Cryptolepine-d(CCTAGG)2
Overview
Cryptolepine, a naturally occurring indoloquinoline alkaloid used as an, antimalarial drug in Central and Western Africa, has been found to bind to, DNA in a formerly unknown intercalation mode. Evidence from competition, dialysis assays demonstrates that cryptolepine is able to bind CG-rich, sequences containing nonalternating CC sites. Here we show that, cryptolepine interacts with the CC sites of the DNA fragment d(CCTAGG)(2), in a base-stacking intercalation mode. This is the first DNA intercalator, complex, from approximately 90 solved by X-ray crystallography, to bind a, nonalternating (pyrimidine-pyrimidine) DNA sequence. The asymmetry of the, drug induces a perfect stacking with the asymmetric site, allowing for the, stability of the complex in the absence of hydrogen bonding interactions., The crystal structure of this antimalarial drug-DNA complex provides, evidence for the first nonalternating intercalation and, as such, provides, a basis for the design of new anticancer or antimalarial drugs.
About this Structure
1K9G is a Protein complex structure of sequences from [1] with DR1 as ligand. Full crystallographic information is available from OCA.
Reference
The antimalarial and cytotoxic drug cryptolepine intercalates into DNA at cytosine-cytosine sites., Lisgarten JN, Coll M, Portugal J, Wright CW, Aymami J, Nat Struct Biol. 2002 Jan;9(1):57-60. PMID:11731803
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